Complete viral genome sequence and discovery of novel viruses by deep sequencing of small RNAs: A generic method for diagnosis, discovery and sequencing of viruses

被引:440
作者
Kreuze, Jan F. [1 ,3 ,4 ]
Perez, Ana [2 ]
Untiveros, Milton [1 ]
Quispe, Dora [1 ]
Fuentes, Segundo [2 ]
Barker, Ian [2 ]
Simon, Reinhard [3 ]
机构
[1] Int Potato Ctr, Germplasm Enhancement & Crop Improved Div, Appl Biotechnol Lab, Lima 12, Peru
[2] Int Potato Ctr, Integrated Crop Management Div, Virol Lab, Lima 12, Peru
[3] Int Potato Ctr, Germplasm Enhancement & Crop Improvement Div, Res Informat Unit, Lima 12, Peru
[4] Swedish Univ Agr Sci, Dept Plant Biol & Forest Genet, SE-75007 Uppsala, Sweden
关键词
siRNA; Deep sequencing; Viral diagnostics; Plant viruses; Virus discovery; Sweetpotato; Badnavirus; Mastrevirus; Potyvirus; Crinivirus; Short sequence assembly; CRINIVIRUS; SUPPRESSOR; INFECTION; PLANT;
D O I
10.1016/j.virol.2009.03.024
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report the first identification of novel viruses, and sequence of an entire vital genome, by a single step of high-throughput parallel sequencing of small RNAs from diseased, as well as symptomless plants. Contigs were assembled from sequenced total siRNA from plants using small sequence assembly software and could positively identify RNA, ssDNA and dsDNA reverse transcribing viruses and in one case spanned the entire genome. The results present a novel approach which cannot only identify known vital pathogens, Occurring at extremely low titers, but also novel viruses, without the necessity of any prior knowledge. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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